Department of Aquatic Sciences and Assessment, Swedish University of Agricultural Sciences, Box 7050, SE-750 07 Uppsala, Sweden.
Environ Pollut. 2012 May;164:102-9. doi: 10.1016/j.envpol.2012.01.024. Epub 2012 Feb 17.
Total mercury concentrations are presented for 19 Swedish watercourses 2000-2010, together with an analysis of factors affecting these concentrations in space and time. Organic matter (OM) measured as absorbance at 420 nm (Abs(420)) and total organic carbon (TOC) were the variables most strongly correlated with THg concentrations in the pooled dataset from all 19 watercourses, explaining 66% and 61% of the variance respectively. The correlation between THg and OM indicates that OM is the main controlling factor independent of geographical variation in Hg deposition, geology, or any other factor evaluated in this study. Despite an increase in TOC concentrations at most sites during the study period, THg increased in only one of the watercourses, and the THg/TOC ratio decreased significantly at six sites. The Abs(420) did not increase like TOC. We suggest that OM-fractions absorbing at 420 nm are more important for Hg mobilization than other OM-fractions.
总汞浓度呈现 19 瑞典河道 2000-2010 年,连同分析这些因素影响的时空浓度。有机物(OM)作为吸光度在 420nm(Abs(420))和总有机碳(TOC)是变量最强烈相关的总汞浓度在 pooled 数据集从所有 19 条河流,分别解释 66%和 61%的方差。汞和有机物之间的相关性表明,有机物是主要控制因素,独立于地理变化汞沉积、地质,或任何其他因素在这项研究中进行了评估。尽管在大多数站点的 TOC 浓度增加,在研究期间,总汞增加了只有一个河道,和总汞/总有机碳的比例显著下降在六个网站。Abs(420)并没有增加像 TOC。我们建议有机物分数吸收在 420nm 是更重要的汞迁移比其他有机物分数。